510(k) K141981 ยท DQY Catheter, Percutaneous
ASAHI FUBUKI 043 / ASAHI FUBUKI
| Applicant | Asahi Intecc Co., Ltd., Baltimore MD, US |
| Decision | Substantially Equivalent, Mar 9, 2015 |
| Received | Jul 21, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141981
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.